Tsuji Y, Hashimoto K, Takeda J, Kakegawa T
Miyazaki Prefectural Hospital.
Nihon Rinsho. 1992 Oct;50(10):2381-5.
We have investigated the cell kinetic effect of four carcinostatic agents (MMC, CDDP, ADR and 5-FU) on the human gastric cancer cell line (KATO-III; signet ring cell carcinoma) by means of flow cytometry (FCM), using bromodeoxyuridine (BrdU) and its monoclonal antibody. Cancer cells in the S phase were first labelled with BrdU and then the bivariate DNA/BrdU distribution was examined to analyze the effect on the cell cycle. Furthermore, cells were reincubated at 24 hours after labelling to evaluate the cell turnover during FCM. MMC, CDDP and ADR assembled the cells into late S phase and G2M phase, while 5-FU assembled them into S phase. after 24 hours, cells with cessation of cell cycle had inhibited their proliferation. We conclude that this technique can be usefully applied as a susceptibility test of carcinostatic agents, since it could define the phase where carcinostatic agents acted on cancer cells.
我们通过流式细胞术(FCM),使用溴脱氧尿苷(BrdU)及其单克隆抗体,研究了四种抗癌药物(丝裂霉素C、顺铂、阿霉素和5-氟尿嘧啶)对人胃癌细胞系(KATO-III;印戒细胞癌)的细胞动力学效应。首先用BrdU标记处于S期的癌细胞,然后检测双变量DNA/BrdU分布,以分析对细胞周期的影响。此外,标记后24小时将细胞重新培养,以评估FCM过程中的细胞更新情况。丝裂霉素C、顺铂和阿霉素使细胞聚集到S期末期和G2M期,而5-氟尿嘧啶使细胞聚集到S期。24小时后,细胞周期停止的细胞其增殖受到抑制。我们得出结论,该技术可有效地用作抗癌药物的敏感性试验,因为它可以确定抗癌药物作用于癌细胞的阶段。